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Catalog Number:
24428
CAS Number:
261165-05-3
+)-(1S,3R-N-Boc-3-aminocyclopentane carboxylic acid
Purity:
≥ 98% (GC)
Synonym(s):
(+)-(1S,3R-N-Boc-β-homocycloleucine, cis-3-N-Boc-amino-cyclopentanecarboxylic acid
Documents
$106.96 /250MG
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Product Information

(+)-(1S,3R)-N-Boc-3-aminocyclopentane carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound features a unique bicyclic structure that enhances its reactivity and selectivity in various chemical reactions. Its N-Boc protecting group is particularly advantageous for facilitating the synthesis of complex molecules, making it an essential building block in the development of pharmaceuticals and agrochemicals. Researchers appreciate its stability under a range of conditions, which allows for straightforward handling and incorporation into diverse synthetic pathways.

In practical applications, this compound has been employed in the synthesis of peptide analogs and other biologically active molecules, showcasing its relevance in drug discovery and development. Its ability to serve as a chiral auxiliary further enhances its utility in asymmetric synthesis, providing researchers with a reliable tool for creating enantiomerically pure compounds. The unique properties of (+)-(1S,3R)-N-Boc-3-aminocyclopentane carboxylic acid make it a valuable asset for professionals seeking efficient and effective solutions in their chemical research and development projects.

Synonyms
(+)-(1S,3R-N-Boc-β-homocycloleucine, cis-3-N-Boc-amino-cyclopentanecarboxylic acid
CAS Number
261165-05-3
Purity
≥ 98% (GC)
Molecular Formula
C11H19NO4
Molecular Weight
229.27
MDL Number
MFCD09992879
PubChem ID
5224745
Appearance
White solid
Conditions
Store at 0-8°C
General Information
Synonyms
(+)-(1S,3R-N-Boc-β-homocycloleucine, cis-3-N-Boc-amino-cyclopentanecarboxylic acid
CAS Number
261165-05-3
Purity
≥ 98% (GC)
Molecular Formula
C11H19NO4
Molecular Weight
229.27
MDL Number
MFCD09992879
PubChem ID
5224745
Appearance
White solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(+)-(1S,3R)-N-Boc-3-aminocyclopentane carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its unique structural properties that enhance bioactivity.
  • Peptide Synthesis: It is commonly used in peptide synthesis as a protecting group for amino acids, allowing for more efficient and selective reactions, which is crucial in developing complex peptide-based drugs.
  • Material Science: The compound can be incorporated into polymers to improve their mechanical properties, making it valuable in creating advanced materials for applications in coatings and adhesives.
  • Bioconjugation: It plays a role in bioconjugation processes, where it can be used to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Research in Organic Chemistry: The compound is a key reagent in organic synthesis, enabling researchers to explore new chemical reactions and develop innovative synthetic pathways that can lead to novel compounds.

Citations